Immunologic Monitoring and Cellular Products Laboratory (IMCPL) IMCPL develops novel procedures and assays to support therapeutic immunotherapy product generation, blood and tissue banking, and immunologic monitoring of patients with cancer at the UPCI.
The specific aims of IMCPL are to: 1) Process blood and tissue and bank biologic specimens from patients participating in IMCPL-related clinical protocols; 2) Facilitate preclinical development, scale-up and preparation of high quality products for cellular, viral and gene therapy of cancer; and 3) Provide serial monitoring of an array of immunologic functions in patients who participate in clinical trials and research protocols at the UPCI. The IMCPL Shared Resource is comprised of three services that include the: a) Tissue Procurement Facility (TPF): The TPF provides specialized blood and tissue processing and banking services for patients participating in clinical protocols. Capabilities include snap freezing, OCT or formalin treatment and single cell digestion and TIL isolation for immediate analysis or banking; b) Cellular Products Laboratory (CPL): The CPL is dedicated to preclinical development, scale-up and preparation of high quality products for cellular and gene therapy of cancer. This includes autologous cells and cell lines, tissue or blood cells modified in vitro for adoptive transfer, and vaccines prepared from peptides, proteins and cells, as well as clinical grade viral vectors; and c) Immunologic Monitoring Laboratory (IML): The IML has responsibility for serial monitoring of an array of immunologic functions in patients who participate in clinical trials and research protocols at the UPCI. The laboratory provides state-of-the-art longitudinal immunologic monitoring with QA/QC, as well as advice on test selection and result interpretation. Together, the IMCPL is a unique laboratory which supports the investigators of the UPCI pursuing cellular therapies, viral products and immune modulation and whose research utilize peripheral blood and tissue from patients on clinical trials. Services are provided by well trained personnel in a certified laboratory with independent QA oversight. The IMCPL enables UPCI researchers and clinicians to perform clinical trials based on autologous and allogeneic cells, to obtain specially processed blood and tumor samples, and to investigate a wide array of immune functions in patients. The IMCPL staff is thoroughly trained and operates in a standardized and quality-assured fashion. During the current project period investigators in all 10 UPCI Research Programs used the IMCPL.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA047904-28
Application #
9114513
Study Section
Subcommittee A - Cancer Centers (NCI-A)
Project Start
Project End
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
28
Fiscal Year
2016
Total Cost
$534,844
Indirect Cost
$187,543
Name
University of Pittsburgh
Department
Type
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Correa, Andres F; Toussi, Amir; Amin, Milon et al. (2018) Small Renal Masses in Close Proximity to the Collecting System and Renal Sinus Are Enriched for Malignancy and High Fuhrman Grade and Should Be Considered for Early Intervention. Clin Genitourin Cancer 16:e729-e733
Wang, Yi-Jun; Fletcher, Rochelle; Yu, Jian et al. (2018) Immunogenic effects of chemotherapy-induced tumor cell death. Genes Dis 5:194-203
Bakkenist, Christopher J; Lee, James J; Schmitz, John C (2018) ATM Is Required for the Repair of Oxaliplatin-Induced DNA Damage in Colorectal Cancer. Clin Colorectal Cancer 17:255-257
Low, Carissa A; Bovbjerg, Dana H; Ahrendt, Steven et al. (2018) Fitbit step counts during inpatient recovery from cancer surgery as a predictor of readmission. Ann Behav Med 52:88-92
Tasdemir, Nilgun; Bossart, Emily A; Li, Zheqi et al. (2018) Comprehensive Phenotypic Characterization of Human Invasive Lobular Carcinoma Cell Lines in 2D and 3D Cultures. Cancer Res 78:6209-6222
Mazharuddin, Samir; Chattopadhyay, Anuja; Levy, Moshe Y et al. (2018) IRF2BP2-RARA t(1;17)(q42.3;q21.2) APL blasts differentiate in response to all-trans retinoic acid. Leuk Lymphoma 59:2246-2249
Basudan, Ahmed; Priedigkeit, Nolan; Hartmaier, Ryan J et al. (2018) Frequent ESR1 and CDK Pathway Copy-Number Alterations in Metastatic Breast Cancer. Mol Cancer Res :
Beumer, Jan H; Chu, Edward; Allegra, Carmen et al. (2018) Therapeutic Drug Monitoring in Oncology: International Association of Therapeutic Drug Monitoring and Clinical Toxicology Recommendations for 5-Fluorouracil Therapy. Clin Pharmacol Ther :
Leng, Shuguang; Diergaarde, Brenda; Picchi, Maria A et al. (2018) Gene Promoter Hypermethylation Detected in Sputum Predicts FEV1 Decline and All-Cause Mortality in Smokers. Am J Respir Crit Care Med 198:187-196
Zhang, Jiliang; Zhang, Shaojuan; Liu, Yang et al. (2018) Combined CB2 receptor agonist and photodynamic therapy synergistically inhibit tumor growth in triple negative breast cancer. Photodiagnosis Photodyn Ther 24:185-191

Showing the most recent 10 out of 1187 publications